Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.10149796T>CCA020399VHLc.473T>C (p.Leu158Pro)
c.350T>C (p.Leu117Pro)
c.*27T>C (p.=)
n.609T>C
ClinVar dbSNP COSMIC
3g.10149796T>ACA16602515VHLc.473T>A (p.Leu158Gln)
c.350T>A (p.Leu117Gln)
c.*27T>A (p.=)
n.609T>A
ClinVar dbSNP COSMIC

Number of alleles fetched